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(S)-6-(4-(benzyloxy)-6-methoxybenzofuran-2-yl)-2-(1-fluoroethyl)imidazo[2,1-b][1,3,4]thiadiazole

Base Information Edit
  • Chemical Name:(S)-6-(4-(benzyloxy)-6-methoxybenzofuran-2-yl)-2-(1-fluoroethyl)imidazo[2,1-b][1,3,4]thiadiazole
  • CAS No.:1476848-37-9
  • Molecular Formula:C22H18FN3O3S
  • Molecular Weight:423.468
  • Hs Code.:
  • Mol file:1476848-37-9.mol
(S)-6-(4-(benzyloxy)-6-methoxybenzofuran-2-yl)-2-(1-fluoroethyl)imidazo[2,1-b][1,3,4]thiadiazole

Synonyms:(S)-6-(4-(benzyloxy)-6-methoxybenzofuran-2-yl)-2-(1-fluoroethyl)imidazo[2,1-b][1,3,4]thiadiazole

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Chemical Property of (S)-6-(4-(benzyloxy)-6-methoxybenzofuran-2-yl)-2-(1-fluoroethyl)imidazo[2,1-b][1,3,4]thiadiazole Edit
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Technology Process of (S)-6-(4-(benzyloxy)-6-methoxybenzofuran-2-yl)-2-(1-fluoroethyl)imidazo[2,1-b][1,3,4]thiadiazole

There total 9 articles about (S)-6-(4-(benzyloxy)-6-methoxybenzofuran-2-yl)-2-(1-fluoroethyl)imidazo[2,1-b][1,3,4]thiadiazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 2 steps
1: N-Bromosuccinimide; sodium hydrogencarbonate / tetrahydrofuran; ethyl acetate
2: dichloromethane; isopropyl alcohol
With N-Bromosuccinimide; sodium hydrogencarbonate; In tetrahydrofuran; dichloromethane; ethyl acetate; isopropyl alcohol;
Guidance literature:
Multi-step reaction with 6 steps
1.1: diisobutylaluminium hydride / dichloromethane; toluene / 3.33 h / -78 °C
1.2: 0.5 h
2.1: caesium carbonate / N,N-dimethyl-formamide / 0.17 h
2.2: 18.08 h / 22 °C / Inert atmosphere
3.1: toluene-4-sulfonic acid / tetrahydrofuran; ethyl acetate / 1 h / 20 °C
4.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.92 h / -78 °C / Inert atmosphere
4.2: 0.42 h / -78 °C / Inert atmosphere
5.1: sodium hydrogencarbonate; N-Bromosuccinimide / tetrahydrofuran / 2.25 h / -20 - 0 °C
6.1: isopropyl alcohol / 18 h / 80 °C
With N-Bromosuccinimide; diisobutylaluminium hydride; sodium hydrogencarbonate; caesium carbonate; toluene-4-sulfonic acid; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; toluene;
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